ATE272062T1 - Spirocyclisch metalloprotease inhibitoren - Google Patents
Spirocyclisch metalloprotease inhibitorenInfo
- Publication number
- ATE272062T1 ATE272062T1 AT97939445T AT97939445T ATE272062T1 AT E272062 T1 ATE272062 T1 AT E272062T1 AT 97939445 T AT97939445 T AT 97939445T AT 97939445 T AT97939445 T AT 97939445T AT E272062 T1 ATE272062 T1 AT E272062T1
- Authority
- AT
- Austria
- Prior art keywords
- spirocyclic
- metalloprotease inhibitors
- metalloprotease
- inhibitors
- spirocyclic metalloprotease
- Prior art date
Links
- 239000003475 metalloproteinase inhibitor Substances 0.000 title 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/10—Spiro-condensed systems
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/56—Ring systems containing three or more rings
- C07D209/96—Spiro-condensed ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Oncology (AREA)
- Virology (AREA)
- Immunology (AREA)
- Hematology (AREA)
- Communicable Diseases (AREA)
- Cardiology (AREA)
- Dermatology (AREA)
- Endocrinology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Reproductive Health (AREA)
- Physical Education & Sports Medicine (AREA)
- Gynecology & Obstetrics (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Obesity (AREA)
- Heart & Thoracic Surgery (AREA)
- Pulmonology (AREA)
- Molecular Biology (AREA)
- Hospice & Palliative Care (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Urology & Nephrology (AREA)
- Neurosurgery (AREA)
- Pregnancy & Childbirth (AREA)
- Rheumatology (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US2476696P | 1996-08-28 | 1996-08-28 | |
| PCT/US1997/014557 WO1998008850A1 (fr) | 1996-08-28 | 1997-08-22 | Inhibiteurs de metalloproteases spirocycliques |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ATE272062T1 true ATE272062T1 (de) | 2004-08-15 |
Family
ID=21822299
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AT97939445T ATE272062T1 (de) | 1996-08-28 | 1997-08-22 | Spirocyclisch metalloprotease inhibitoren |
Country Status (29)
| Country | Link |
|---|---|
| US (1) | US6015912A (fr) |
| EP (1) | EP0927183B1 (fr) |
| JP (2) | JP3495376B2 (fr) |
| KR (1) | KR100326611B1 (fr) |
| CN (1) | CN1105723C (fr) |
| AR (1) | AR009358A1 (fr) |
| AT (1) | ATE272062T1 (fr) |
| AU (1) | AU736238B2 (fr) |
| BR (1) | BR9713178A (fr) |
| CA (1) | CA2264044A1 (fr) |
| CO (1) | CO4900045A1 (fr) |
| CZ (1) | CZ63799A3 (fr) |
| DE (1) | DE69730033T2 (fr) |
| DK (1) | DK0927183T3 (fr) |
| ES (1) | ES2225983T3 (fr) |
| HU (1) | HUP9904694A3 (fr) |
| ID (1) | ID19418A (fr) |
| IL (1) | IL128667A (fr) |
| NO (1) | NO315373B1 (fr) |
| NZ (1) | NZ334257A (fr) |
| PE (1) | PE107798A1 (fr) |
| PL (1) | PL331920A1 (fr) |
| PT (1) | PT927183E (fr) |
| RU (1) | RU2203274C2 (fr) |
| SK (1) | SK284041B6 (fr) |
| TR (1) | TR199900429T2 (fr) |
| TW (1) | TW581761B (fr) |
| WO (1) | WO1998008850A1 (fr) |
| ZA (1) | ZA977699B (fr) |
Families Citing this family (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20030206874A1 (en) * | 1996-11-21 | 2003-11-06 | The Proctor & Gamble Company | Promoting whole body health |
| CN1265647A (zh) | 1997-07-31 | 2000-09-06 | 普罗克特和甘保尔公司 | 无环金属蛋白酶抑制剂 |
| US6410580B1 (en) | 1998-02-04 | 2002-06-25 | Novartis Ag | Sulfonylamino derivatives which inhibit matrix-degrading metalloproteinases |
| ID24957A (id) | 1998-02-04 | 2000-08-31 | Novartis Ag | Turunan sulfonilamino yang menginhibisi metaloproteinase penurun matriks |
| US6846478B1 (en) | 1998-02-27 | 2005-01-25 | The Procter & Gamble Company | Promoting whole body health |
| US6197974B1 (en) * | 1998-10-26 | 2001-03-06 | Abbott Laboratories | Enantioselective synthesis of 3-aminopyrrolidines |
| US6858598B1 (en) | 1998-12-23 | 2005-02-22 | G. D. Searle & Co. | Method of using a matrix metalloproteinase inhibitor and one or more antineoplastic agents as a combination therapy in the treatment of neoplasia |
| JP2002538146A (ja) | 1999-03-03 | 2002-11-12 | ザ プロクター アンド ギャンブル カンパニー | ジヘテロ−置換メタロプロテアーゼ阻害剤 |
| CZ20013176A3 (cs) | 1999-03-03 | 2002-04-17 | The Procter & Gamble Company | Sloučenina vytvářející inhibitor metaloproteinasy, farmaceutický prostředek, způsob přípravy léčiva a léčivo |
| US8283135B2 (en) * | 2000-06-30 | 2012-10-09 | The Procter & Gamble Company | Oral care compositions containing combinations of anti-bacterial and host-response modulating agents |
| WO2002002128A2 (fr) * | 2000-06-30 | 2002-01-10 | The Procter & Gamble Company | Renforcement global de l'organisme |
| DE60134854D1 (de) * | 2000-06-30 | 2008-08-28 | Procter & Gamble | Orale zubereitungen, die wirtsantwortmodulierenden wirkstoffe enthalten |
| FR2818643B1 (fr) * | 2000-12-22 | 2003-02-07 | Servier Lab | Nouveaux inhibiteurs de metalloproteases, leur procede de preparation et les compositions pharmaceutiques que les contiennent |
| WO2003016248A2 (fr) | 2001-08-17 | 2003-02-27 | Bristol-Myers Squibb Company Patent Department | Hydroxamates bicycliques utilises comme inhibiteurs de metalloproteinases matricielles et/ou enzyme de conversion du tnf-$g(a) (tace) |
| AU2004233863B2 (en) | 2003-04-24 | 2010-06-17 | Incyte Holdings Corporation | Aza spiro alkane derivatives as inhibitors of metalloproteases |
| DE102004004974A1 (de) * | 2004-01-31 | 2005-08-18 | Aventis Pharma Deutschland Gmbh | Thieno-Iminosäure-Derivate als Inhibitoren von Matrix-Metalloproteinasen |
| SI2032535T1 (sl) * | 2006-06-01 | 2012-12-31 | Sanofi | Spirociklični nitrili kot proteazni inhibitorji |
| NZ579295A (en) * | 2007-02-27 | 2012-03-30 | Vertex Pharma | Inhibitors of serine proteases |
| CA2676933C (fr) * | 2007-02-28 | 2015-09-29 | Leo Pharma A/S | Nouveaux inhibiteurs de la phosphodiesterase |
| AU2010289762B2 (en) | 2009-09-04 | 2015-06-11 | Janssen Pharmaceuticals, Inc. | Chemical compounds |
| WO2012123298A1 (fr) | 2011-03-11 | 2012-09-20 | F. Hoffmann-La Roche Ag | Composés antiviraux |
| RU2523284C9 (ru) * | 2012-05-31 | 2014-10-10 | Автономная Некоммерческая Организация "Научно-Исследовательский Центр Биотехнологии Антибиотиков И Других Биологически Активных Веществ "Биоан" | Способ модификации макролидного антибиотика олигомицина а с помощью реакции [3+2]-диполярного циклоприсоединения азида и алкинов. 33-дезокис-33-(триазол-1-ил)-олигомицины а и их биологическая активность |
| UA119247C2 (uk) | 2013-09-06 | 2019-05-27 | РОЙВЕНТ САЙЕНСИЗ ҐмбГ | Спіроциклічні сполуки як інгібітори триптофангідроксилази |
| US9611201B2 (en) | 2015-03-05 | 2017-04-04 | Karos Pharmaceuticals, Inc. | Processes for preparing (R)-1-(5-chloro-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanol and 1-(5-chloro-[1,1′-biphenyl]-2-yl)-2,2,2-trifluoroethanone |
| AR110150A1 (es) * | 2016-11-09 | 2019-02-27 | Roivant Sciences Gmbh | Procesos para la preparación de inhibidores de tph1 |
Family Cites Families (30)
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| NL6818875A (fr) * | 1968-01-24 | 1969-07-28 | ||
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| US4555579A (en) * | 1983-03-24 | 1985-11-26 | E. R. Squibb & Sons, Inc. | Dioxolenylmethyl ester prodrugs of phosphinic acid ace inhibitors |
| US4709046A (en) * | 1983-05-09 | 1987-11-24 | E. R. Squibb & Sons, Inc. | Acylmercaptoalkanoyl and mercaptoalkanoyl spiro compounds |
| EP0189370A3 (fr) * | 1985-01-16 | 1988-01-27 | Sandoz Ag | Spiro-dioxolanes, -dithiolanes et -oxothiolanes |
| DK167393B1 (da) * | 1985-12-30 | 1993-10-25 | Roussel Uclaf | 1-sulfonyl-2-oxo-pyrrolidinderivater, deres fremstilling og farmaceutiske praeparater med indhold deraf |
| GB8601368D0 (en) * | 1986-01-21 | 1986-02-26 | Ici America Inc | Hydroxamic acids |
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| DD298639A5 (de) * | 1989-12-21 | 1992-03-05 | Institut Fuer Chemische Technologie,De | Verfahren zur herstellung von sulfobetainsubstituierten alpha-sulfonyl-carbonsaeuren aus diallylammoniumsalzen |
| DE4011172A1 (de) * | 1990-04-06 | 1991-10-10 | Degussa | Verbindungen zur bekaempfung von pflanzenkrankheiten |
| US5183900A (en) * | 1990-11-21 | 1993-02-02 | Galardy Richard E | Matrix metalloprotease inhibitors |
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| IL98681A (en) * | 1991-06-30 | 1997-06-10 | Yeda Rehovot And Dev Company L | Pharmaceutical compositions comprising hydroxamate derivatives for iron removal from mammalian cells and from pathogenic organisms and some novel hydroxamate derivatives |
| DE4127842A1 (de) * | 1991-08-22 | 1993-02-25 | Rhone Poulenc Rorer Gmbh | 5-((omega)-arylalky)-2-thienyl alkansaeuren, ihre salze und/oder ihre derivate |
| JPH05125029A (ja) * | 1991-11-06 | 1993-05-21 | Yamanouchi Pharmaceut Co Ltd | 新規なアミド化合物又はその塩 |
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| AU3899193A (en) * | 1992-04-07 | 1993-11-08 | British Bio-Technology Limited | Hydroxamic acid based collagenase and cytokine inhibitors |
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1997
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